MX2009002707A - Azole nucleosides and use as inhibitors of rna and dna varial polymerases. - Google Patents
Azole nucleosides and use as inhibitors of rna and dna varial polymerases.Info
- Publication number
- MX2009002707A MX2009002707A MX2009002707A MX2009002707A MX2009002707A MX 2009002707 A MX2009002707 A MX 2009002707A MX 2009002707 A MX2009002707 A MX 2009002707A MX 2009002707 A MX2009002707 A MX 2009002707A MX 2009002707 A MX2009002707 A MX 2009002707A
- Authority
- MX
- Mexico
- Prior art keywords
- heterocyclo
- aryl
- cycloalkyl
- alkyl
- cycloalkenyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/044—Pyrrole radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/056—Triazole or tetrazole radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
- C07H5/06—Aminosugars
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Virology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Azole nucleosides represented by the formulae (I) and (II); wherein A = C or N B = C or N X = H; C1-C6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo, halogen such as F, C1, Br and I; OH, NH2, NH-(C1-C6 alkyl, cycloalkyl, aryl, or heterocyclo); Z = H; C1-C6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo, halogen such as F, Cl, Br, I; OH, NH2, NH-(C1-C6 alkyl, cycloalkyl, aryl, or heterocyclo; E= (CH2)HONHR1; n is an integer from 0-6 and more typically 0-3; R1= aryl or heterocyclo; each of W, Y, R is individually selected from the group consisting of H; C1-C6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo; halogen such as F, Cl, Br, and I; O, OH, Oalkyl, Oaryl, NH2, NH-(C1-C6 alkyl, cycloalkyl, aryl, or heterocyclo); provided that at least one of W, Y, and R is other than H and wherein both W and Y together can be =O; and each D individually is OH, Oalkyl, Oaryl, Fl and H;pharmaceutically acceptable salts thereof, prodrugs thereof and mixtures thereof are provided. Compounds of this disclosure are useful as inhibitors of viral RNA and DNA polymerases such as, but not limited to, Influenza, Hantaan Virus, Crimean Congo hemorrhagic fever virus, hepatitis B, hepatitis C, Polio, Coxsackie A and B, Rhino, Echo, orthopoxvirus (small pox), HIV, Ebola, and West Nile virus polymerases; and especially orthopoxvirus, HIV, and hepatitis B.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US84339806P | 2006-09-11 | 2006-09-11 | |
PCT/US2007/078139 WO2008067002A2 (en) | 2006-09-11 | 2007-09-11 | Azole nucleosides and use as inhibitors of rna and dna varial polymerases |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009002707A true MX2009002707A (en) | 2009-11-26 |
Family
ID=39468551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009002707A MX2009002707A (en) | 2006-09-11 | 2007-09-11 | Azole nucleosides and use as inhibitors of rna and dna varial polymerases. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20100129317A1 (en) |
EP (1) | EP2061316A4 (en) |
JP (1) | JP2010502748A (en) |
KR (1) | KR20090094800A (en) |
CN (1) | CN101511185A (en) |
AU (1) | AU2007325551A1 (en) |
CA (1) | CA2663618A1 (en) |
EA (1) | EA016830B1 (en) |
IL (1) | IL197415A0 (en) |
MX (1) | MX2009002707A (en) |
WO (1) | WO2008067002A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0714649D0 (en) * | 2007-07-27 | 2007-09-05 | Univ Leuven Kath | Novel viral replication inhibitors |
EP2113508A1 (en) * | 2008-04-30 | 2009-11-04 | INSERM (Institut National de la Santé et de la Recherche Medicale) | Novel triazole nucleoside derivatives, their preparation and their application in therapeutics |
GB0815968D0 (en) * | 2008-09-03 | 2008-10-08 | Angeletti P Ist Richerche Bio | Antiviral agents |
RS56870B1 (en) | 2010-10-15 | 2018-04-30 | Biocryst Pharm Inc | Pyrrolopyrimidine derivatives for use in the treatment of viral infections |
AR090699A1 (en) | 2012-04-18 | 2014-12-03 | Biocryst Pharm Inc | INHIBITING COMPOUNDS OF VIRAL POLYMERASE RNA ACTIVITY |
CA3016588A1 (en) | 2016-03-06 | 2017-09-14 | Biocryst Pharmaceuticals, Inc. | Methods and compositions for treatment of zika virus infection |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3968103A (en) * | 1972-09-28 | 1976-07-06 | Icn Pharmaceuticals, Inc. | 1,2,3-Triazole nucleosides |
JPS6426593A (en) * | 1987-07-21 | 1989-01-27 | Asahi Glass Co Ltd | Nucleoside derivative |
US4925930A (en) * | 1988-11-02 | 1990-05-15 | Nucleic Acid Research Institute | Synthesis and anti-leukemic activity of alkyl-1-(β-D-ribofuranosyl)[1,2,4]triazole-3-carboximidates |
US4992426A (en) * | 1989-02-27 | 1991-02-12 | Nucleic Acid Research Institute | Antiparasitic 5'-sulfamoyl nucleosides |
US6358931B1 (en) * | 1990-01-11 | 2002-03-19 | Isis Pharmaceuticals, Inc. | Compositions and methods for modulating RNA |
US7037646B1 (en) * | 1990-01-11 | 2006-05-02 | Isis Pharmaceuticals, Inc. | Amine-derivatized nucleosides and oligonucleosides |
US6060592A (en) * | 1990-01-11 | 2000-05-09 | Isis Pharmaceuticals, Inc. | Pyrimidine nucleoside compounds and oligonucleoside compounds containing same |
US6339066B1 (en) * | 1990-01-11 | 2002-01-15 | Isis Pharmaceuticals, Inc. | Antisense oligonucleotides which have phosphorothioate linkages of high chiral purity and which modulate βI, βII, γ, δ, Ε, ζ and η isoforms of human protein kinase C |
US6153737A (en) * | 1990-01-11 | 2000-11-28 | Isis Pharmaceuticals, Inc. | Derivatized oligonucleotides having improved uptake and other properties |
US6783931B1 (en) * | 1990-01-11 | 2004-08-31 | Isis Pharmaceuticals, Inc. | Amine-derivatized nucleosides and oligonucleosides |
US5777100A (en) * | 1990-08-10 | 1998-07-07 | Gensia Inc. | AICA riboside analogs |
US6262241B1 (en) * | 1990-08-13 | 2001-07-17 | Isis Pharmaceuticals, Inc. | Compound for detecting and modulating RNA activity and gene expression |
CA2133355A1 (en) * | 1993-10-04 | 1995-04-05 | Itaru Nitta | Method for producing polypeptide |
US5767097A (en) * | 1996-01-23 | 1998-06-16 | Icn Pharmaceuticals, Inc. | Specific modulation of Th1/Th2 cytokine expression by ribavirin in activated T-lymphocytes |
GB9602028D0 (en) * | 1996-02-01 | 1996-04-03 | Amersham Int Plc | Nucleoside analogues |
IL129126A0 (en) * | 1996-10-16 | 2000-02-17 | Icn Pharmaceuticals | Monocyclic l-nucleosides analogs and uses thereof |
US6312662B1 (en) * | 1998-03-06 | 2001-11-06 | Metabasis Therapeutics, Inc. | Prodrugs phosphorus-containing compounds |
US6277830B1 (en) * | 1998-10-16 | 2001-08-21 | Schering Corporation | 5′-amino acid esters of ribavirin and the use of same to treat hepatitis C with interferon |
EP1244356A4 (en) * | 1999-12-23 | 2003-03-19 | Icn Pharmaceuticals | Compositions and methods for l-nucleosides, l-nucleotides, and their analogs |
US6495677B1 (en) * | 2000-02-15 | 2002-12-17 | Kanda S. Ramasamy | Nucleoside compounds |
FR2810322B1 (en) * | 2000-06-14 | 2006-11-10 | Pasteur Institut | COMBINATORY PRODUCTION OF NUCLEOTIDE AND NUCLEOTIDE ANALOGUES (XiTP) |
US6900298B2 (en) * | 2002-02-12 | 2005-05-31 | Mitsubishi Chemical Corporation | Process for producing nucleic acid derivative |
CA2477795A1 (en) * | 2002-02-28 | 2003-09-12 | Kandasamy Sakthivel | Nucleoside 5'-monophosphate mimics and their prodrugs |
WO2004084796A2 (en) * | 2003-03-28 | 2004-10-07 | Pharmasset Ltd. | Compounds for the treatment of flaviviridae infections |
CA2537849A1 (en) * | 2003-09-11 | 2005-03-17 | F. Hoffmann-La Roche Ag | Process for preparing antiviral nucleoside derivatives |
US7348146B2 (en) * | 2003-10-02 | 2008-03-25 | Epoch Biosciences, Inc. | Single nucleotide polymorphism analysis of highly polymorphic target sequences |
-
2007
- 2007-09-11 WO PCT/US2007/078139 patent/WO2008067002A2/en active Application Filing
- 2007-09-11 EA EA200970261A patent/EA016830B1/en not_active IP Right Cessation
- 2007-09-11 EP EP07871070A patent/EP2061316A4/en not_active Withdrawn
- 2007-09-11 KR KR1020097005086A patent/KR20090094800A/en not_active Application Discontinuation
- 2007-09-11 MX MX2009002707A patent/MX2009002707A/en not_active Application Discontinuation
- 2007-09-11 US US12/440,697 patent/US20100129317A1/en not_active Abandoned
- 2007-09-11 JP JP2009527620A patent/JP2010502748A/en active Pending
- 2007-09-11 CA CA002663618A patent/CA2663618A1/en not_active Abandoned
- 2007-09-11 AU AU2007325551A patent/AU2007325551A1/en not_active Abandoned
- 2007-09-11 CN CNA2007800337456A patent/CN101511185A/en active Pending
-
2009
- 2009-03-05 IL IL197415A patent/IL197415A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2008067002A3 (en) | 2008-11-06 |
WO2008067002A2 (en) | 2008-06-05 |
KR20090094800A (en) | 2009-09-08 |
WO2008067002A8 (en) | 2008-09-12 |
CN101511185A (en) | 2009-08-19 |
EP2061316A2 (en) | 2009-05-27 |
JP2010502748A (en) | 2010-01-28 |
CA2663618A1 (en) | 2008-06-05 |
AU2007325551A1 (en) | 2008-06-05 |
EA200970261A1 (en) | 2010-02-26 |
IL197415A0 (en) | 2009-12-24 |
US20100129317A1 (en) | 2010-05-27 |
EP2061316A4 (en) | 2011-08-24 |
EA016830B1 (en) | 2012-07-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |